CRYAB

CRYAB (Crystallin Alpha B) is a protein that in humans is encoded by the CRYAB gene. It is a member of the small heat shock protein (sHSP) family and plays a crucial role in maintaining the structural integrity of the lens in the eye, as well as in other tissues.

Function

CRYAB functions as a molecular chaperone, preventing the aggregation of denatured proteins. It is involved in the cellular response to stress and helps in the maintenance of cellular homeostasis. CRYAB is expressed in various tissues, including the lens of the eye, heart, skeletal muscle, and kidney.

Structure

The CRYAB protein is composed of 175 amino acids and has a molecular weight of approximately 20 kDa. It forms large oligomeric complexes that are essential for its chaperone activity. The protein structure includes an alpha-crystallin domain, which is characteristic of the small heat shock protein family.

Clinical Significance

Mutations in the CRYAB gene have been associated with several diseases, including cardiomyopathy, cataract, and myopathy. These mutations can lead to the misfolding and aggregation of proteins, resulting in cellular dysfunction and disease.

Cardiomyopathy

CRYAB mutations can cause dilated cardiomyopathy and restrictive cardiomyopathy. These conditions are characterized by the weakening of the heart muscle, leading to heart failure and other complications.

Cataract

Mutations in CRYAB are linked to congenital cataracts, which are characterized by the clouding of the lens in the eye, leading to impaired vision or blindness.

Myopathy

CRYAB-related myopathy is a muscle disorder that can cause muscle weakness and degeneration. It is often associated with the accumulation of protein aggregates in muscle cells.

Expression

CRYAB is highly expressed in the lens of the eye, where it constitutes a significant portion of the total protein content. It is also expressed in other tissues, including the heart, skeletal muscle, and kidney.

Interactions

CRYAB interacts with various other proteins, including other small heat shock proteins, to perform its chaperone functions. It also interacts with cytoskeletal proteins, which helps in maintaining cellular structure and integrity.

Related Pages

• Small heat shock protein
• Cardiomyopathy
• Cataract
• Myopathy
• Lens (anatomy)
• Protein folding
• Molecular chaperone

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